Transcript #00023119 (NM_030751.5, ZEB1 gene)

Transcript name transcript variant 2
Gene name ZEB1 (zinc finger E-box binding homeobox 1)
Chromosome 10
Transcript - NCBI ID NM_030751.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_110378.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

79 entries on 1 page. Showing entries 1 - 79.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. _1_9_ c.0 r.0 p.0
+/. _1_9_ c.0 r.0 p.0
+/. - c.1A>G r.(?) p.(Met1?)
+/. - c.2T>G r.(?) p.(Met1?)
+/. - c.3G>T r.(?) p.(Met1?)
?/. - c.15del r.(?) p.(Arg6GlyfsTer22)
-?/. - c.17G>A r.(?) p.(Arg6Lys)
+/. - c.34C>T r.(?) p.(Gln12*)
?/. - c.77_82del r.(?) p.(Val26_Val27del)
?/. - c.77_82del r.(?) p.(Val26_Val27del)
+?/. 2 c.101A>G r.(?) p.(Lys34Arg)
?/. - c.146A>T r.(?) p.(Asp49Val)
?/. - c.170C>T r.(?) p.(Pro57Leu)
-?/. - c.180C>T r.(?) p.(Asp60=)
+/. - c.233A>C r.(?) p.(Asn78Thr)
+/. 3i_9_ c.319+28_*39555delinsACACACAC r.? p.?
+/. - c.358C>T r.(?) p.(Gln120Ter)
+/. - c.449del r.(?) p.(Gly150Alafs*36)
+/. - c.449del r.(?) p.(Gly150Alafs*36)
-?/. - c.481+7G>T r.(=) p.(=)
+/. - c.627del r.(?) p.(Phe209Leufs*11)
+/. - c.640C>T r.(?) p.(Gln214*)
?/. - c.650G>A r.(?) p.(Arg217His)
?/. - c.657G>T r.(?) p.(Met219Ile)
+/. - c.672del r.(?) p.(Gly225Glufs*7)
-/. - c.685-15G>A r.(=) p.(=)
+/. - c.685-2A>G r.spl p.(?)
+/. - c.689_690del r.(?) p.(His230Argfs*7)
-?/. - c.696G>A r.(?) p.(Thr232=)
+/. - c.698dup r.(?) p.(Ser234Valfs*4)
-?/. - c.789T>C r.(?) p.(Ser263=)
-?/. - c.791-6_791-3del r.spl? p.?
+/. - c.929dup r.(?) p.(Cys311Valfs*25)
+/. - c.973C>T r.(?) p.(Arg325*)
?/. - c.985C>T r.(?) p.(Arg329Trp)
+/. - c.1124del r.(?) p.(Phe375Serfs*31)
+/. - c.1176dup r.(?) p.(Ala393Serfs*19)
+/. - c.1332_1335del r.(?) p.(Ile444Metfs*48)
+/. - c.1348C>T r.(?) p.(Gln450*)
+/. - c.1387_1390del r.(?) p.(Pro463Trpfs*29)
-?/. - c.1438G>C r.(?) p.(Glu480Gln)
?/. - c.1438G>C r.(?) p.(Glu480Gln)
+/. - c.1440_1441del r.(?) p.(Gln481AlafsTer2)
+/. - c.1482dup r.(?) p.(Glu495Argfs*10)
?/. - c.1495G>A r.(?) p.(Ala499Thr)
+/. - c.1569del r.(?) p.(Val526*)
+/. - c.1576del r.(?) p.(Val526Ter)
+/. - c.1576dup r.(?) p.(Val526Glyfs*3)
+/. - c.1576dup r.(?) p.(Val526Glyfs*3)
+/. - c.1576dup r.(?) p.(Val526Glyfs*3)
+/. - c.1576dup r.(?) p.(Val526Glyfs*3)
+/. - c.1669C>T r.(?) p.(Gln557*)
+/. - c.1717_1718del r.(?) p.(Val573Phefs*12)
+/. - c.1751del r.(?) p.(Pro584Leufs*6)
?/. - c.1775T>C r.(?) p.(Leu592Pro)
-?/. - c.1794A>G r.(?) p.(Ala598=)
+/. - c.1913_1914del r.(?) p.(Ser638Cysfs*5)
-?/. - c.1974C>G r.(?) p.(Asn658Lys)
+/. - c.2034_2035del r.(?) p.(Pro680PhefsTer5)
+?/. - c.2058_2062dup r.(?) p.(Val688Alafs*23)
+/. - c.2157C>G r.(?) p.(Tyr719*)
+/. - c.2182G>T r.(?) p.(Glu728*)
+/. - c.2249C>A r.(?) p.(Ser750*)
?/. - c.2251A>G r.(?) p.(Thr751Ala)
+/. - c.2324dup r.(?) p.(Glu776Glyfs*44)
?/. - c.2416A>G r.(?) p.(Thr806Ala)
-?/. - c.2519A>C r.(?) p.(Gln840Pro)
?/. - c.2519A>C r.(?) p.(Gln840Pro)
+/. - c.2519A>C r.(?) p.(Gln840Pro)
+/. - c.2617dup r.(?) p.(Thr873Asnfs*2)
+/. - c.2650del r.(?) p.(Gln884Argfs*37)
?/. - c.2668A>C r.(?) p.(Thr890Pro)
-?/. - c.2703T>C r.(?) p.(Asn901=)
+/. - c.2916_2917del r.(?) p.(Gly973Valfs*14)
+/. - c.2990_2991del r.(?) p.(Glu997Alafs*7)
?/. - c.3073_3080del r.(?) p.(Arg1025Phefs*7)
-?/. - c.3090G>A r.(?) p.(Arg1030=)
+/. - c.3116_3117del r.(?) p.(Glu1039Glyfs*6)
-?/. - c.3207_3209del r.(?) p.(Glu1071del)
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